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FDA 510(k)

Vitrea Software Toshiba Package; VSTP-001A

K-Number: K171222 · 2017-06-08

ApplicantToshibamedical Systems Corporation
Decision Date2017-06-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Vitrea Software Toshiba Package; VSTP-001A is the device name listed in this FDA 510(k) record. The listed applicant is Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2017-06-08 under 510(k) number K171222. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vitrea Software Toshiba Package; VSTP-001A?

Vitrea Software Toshiba Package; VSTP-001A is a medical device that received FDA 510(k) clearance on 2017-06-08. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K171222.

When did Vitrea Software Toshiba Package; VSTP-001A receive FDA 510(k) clearance?

Vitrea Software Toshiba Package; VSTP-001A received FDA 510(k) clearance on 2017-06-08, under 510(k) number K171222.

Who is the listed applicant for Vitrea Software Toshiba Package; VSTP-001A?

The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vitrea Software Toshiba Package; VSTP-001A?

The FDA product code for Vitrea Software Toshiba Package; VSTP-001A is LLZ.

Other records listing Toshibamedical Systems Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K173962Viamo c100 TUS-VC100 Diagnostic Ultrasound SystemK173468Aquilion Precision (TSX-304A/2) V8.6 with FIRST 3.0K173088Vitrea Software Toshiba Package VSTP-001AK173382Vantage Galan 3T, V4.6K173090Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4K172863Infinix-i, INFX-8000V, V7.0

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Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLCK261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific CorporationK262143ImageGrid StreamVueCandelis, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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